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Results: 1 to 5 of 5

Tests names and labsConditionsGenes, analytes, and microbesMethods

Leber congenital amaurosis 18, 608133, Autosomal recessive, Autosomal dominant (Retinitis pigmentosa) (MLPA)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Leber congenital amaurosis 18, 608133, Autosomal recessive, Autosomal dominant (Retinitis pigmentosa) (PRPH2 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Retinitis pigmentosa 7, digenic, 608133, Autosomal recessive, Autosomal dominant (Retinitis pigmentosa) (ROM1 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Retinitis pigmentosa 7 and digenic, 608133, Autosomal recessive, Autosomal dominant; RP7 (Retinitis pigmentosa) (MLPA)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Retinitis pigmentosa 7 and digenic, 608133, Autosomal recessive, Autosomal dominant; RP7 (Retinitis pigmentosa) (PRPH2 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Results: 1 to 5 of 5

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